Clinical Research Assistant II — Data & Trials Support

The University of Texas Southwestern Medical Center; Dallas (TX); Sur place; USD 55 000 - 75 000; Plein temps

Avantages offerts par ce poste

PPO medical plan day one

100% coverage preventive care

Paid Time Off day one

TRS retirement

Paid Parental Leave

Wellness programs

Tuition Reimbursement

PSLF Qualified Employer

Résumé du poste

The University of Texas Southwestern Medical Center in Dallas seeks a Clinical Research Data Coordinator to manage data for local and national studies under supervision. This role supports protocol tasks, data quality, and regulatory activities within a clinical research setting.

You will assist with patient screening, data entry, documentation, and coordinating with the research team to ensure compliance and study timelines. Strong attention to detail is essential.

Qualifications

• Experience with clinical study data management.
• Ability to review medical records for eligibility.
• Familiarity with data collection systems and regulatory requirements.

Responsabilités

• Manage data entry into case report forms and systems.
• Maintain study documentation and data integrity.
• Support regulatory submissions and audits.
• Recruit and screen participants under supervision.
• Assist with protocol tasks and QA/QC checks.
• Help prepare annual reports and IRB modifications.
• Assist with study closeout activities.

Connaissances

Data management

Organizational skills

Communication skills

PHI/compliance

InterviewingParticipants

Teamwork

Formation

High School Diploma / Associate's / Bachelor's in medical or science field

Description du poste

The University of Texas Southwestern Medical Center in Dallas seeks a Clinical Research Data Coordinator to manage data for local and national studies under supervision. This role supports protocol tasks, data quality, and regulatory activities within a clinical research setting.

You will assist with patient screening, data entry, documentation, and coordinating with the research team to ensure compliance and study timelines. Strong attention to detail is essential.